GapMind for catabolism of small carbon sources

 

Alignments for a candidate for araZsh in Herbaspirillum seropedicae SmR1

Align Inner-membrane translocator (characterized, see rationale)
to candidate HSERO_RS05325 HSERO_RS05325 ribose ABC transporter permease

Query= uniprot:A0KWY7
         (320 letters)



>FitnessBrowser__HerbieS:HSERO_RS05325
          Length = 328

 Score =  159 bits (402), Expect = 9e-44
 Identities = 100/304 (32%), Positives = 169/304 (55%), Gaps = 7/304 (2%)

Query: 8   PLWITASLLLTMFLVGTFQFDGFASGRVVTNLLRDNAFLLITALGMTLVIISGGIDLSVG 67
           PL +  + L+ + L+     D F +     N+LR  + + I A+GM+ VI++GGIDLSVG
Sbjct: 28  PLALPLAGLVVVSLLMGLASDNFFTLSNWFNVLRQVSIVGILAVGMSFVILTGGIDLSVG 87

Query: 68  AVIALSGVVTSLLITEYQWHPLLAFVVILPLGTLFGALMGTIIHVYKLQPFIVTLAGMFL 127
           A +AL+G +++ LI        LA +  + L T  G L G ++   ++   IVTLA M +
Sbjct: 88  AAMALAGTISAGLIVNSGLPAPLALLCGVGLATCIGLLNGALVAWGRMPAIIVTLATMGV 147

Query: 128 ARGLATTLSEESIAIDHPFYDAVAEMSIALPGN-GALDLSSLIFILFFVIIAVVMHYTRF 186
           ARG+    S       +P       +S    G  G + +  ++ ++ + +  +++  T F
Sbjct: 148 ARGVGLIYSG-----GYPISGLPGWISWFGVGRIGMVPVPVILMLIVYALAWLLLQRTAF 202

Query: 187 GTNVYAIGGNQHSAELMGISIAKTTISIYAISSFLATLAGIVFTFYTFSGYALGAIGVEL 246
           G +VYAIGGN+ +A L G+   +  +++YAIS F + LA I+ T    SG     +G EL
Sbjct: 203 GRHVYAIGGNEMAARLSGVKTTRIKLAVYAISGFTSGLAAIILTGRLMSGQPNAGVGFEL 262

Query: 247 DAIAAVVIGGTLLTGGSGFVLGTVLGVILMGVIQTYITFDGSLSSWWTKIVIGLLLFFFI 306
           DAIAAVV+GGT + GG G V+GT++G +L+G++   +   G ++ +   I+ G+++   I
Sbjct: 263 DAIAAVVLGGTAIAGGRGLVVGTLIGAVLLGILNNGLNLMG-INPYLQDIIRGVIILLAI 321

Query: 307 LLQK 310
            + +
Sbjct: 322 YIAR 325


Lambda     K      H
   0.330    0.145    0.424 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 379
Number of extensions: 24
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 320
Length of database: 328
Length adjustment: 28
Effective length of query: 292
Effective length of database: 300
Effective search space:    87600
Effective search space used:    87600
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory